Canonical Allele Identifier: PA2825135117
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2700979
ClinVar RCV Id: RCV003501092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Leu239Pro
CA411143815
NM_000268.4:c.716T>C